CA1288087C - Methode et composition pour separer le sulfure d'hydrogene present dans des debits gazeux - Google Patents
Methode et composition pour separer le sulfure d'hydrogene present dans des debits gazeuxInfo
- Publication number
- CA1288087C CA1288087C CA000535735A CA535735A CA1288087C CA 1288087 C CA1288087 C CA 1288087C CA 000535735 A CA000535735 A CA 000535735A CA 535735 A CA535735 A CA 535735A CA 1288087 C CA1288087 C CA 1288087C
- Authority
- CA
- Canada
- Prior art keywords
- polyvalent metal
- metal chelate
- chelate
- amount
- aqueous alkaline
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000000034 method Methods 0.000 title claims abstract description 56
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 title claims abstract description 48
- 229910000037 hydrogen sulfide Inorganic materials 0.000 title claims abstract description 45
- 239000000203 mixture Substances 0.000 title claims abstract description 21
- 229910052751 metal Inorganic materials 0.000 claims abstract description 123
- 239000002184 metal Substances 0.000 claims abstract description 123
- 239000013522 chelant Substances 0.000 claims abstract description 122
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 65
- 230000003647 oxidation Effects 0.000 claims abstract description 64
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 46
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 36
- 239000011593 sulfur Substances 0.000 claims abstract description 36
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000012670 alkaline solution Substances 0.000 claims abstract description 32
- RWSOTUBLDIXVET-UHFFFAOYSA-M hydrosulfide Chemical compound [SH-] RWSOTUBLDIXVET-UHFFFAOYSA-M 0.000 claims abstract description 27
- 239000000243 solution Substances 0.000 claims abstract description 25
- 238000005201 scrubbing Methods 0.000 claims abstract description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 75
- 229910052742 iron Inorganic materials 0.000 claims description 37
- 239000007789 gas Substances 0.000 claims description 30
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- 239000001301 oxygen Substances 0.000 claims description 22
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 20
- 239000002253 acid Substances 0.000 claims description 19
- 239000004215 Carbon black (E152) Substances 0.000 claims description 9
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- 239000006172 buffering agent Substances 0.000 claims description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- 238000011084 recovery Methods 0.000 claims description 6
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical group C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 239000011733 molybdenum Substances 0.000 claims description 3
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- 239000011135 tin Substances 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 239000002737 fuel gas Substances 0.000 claims description 2
- 239000003345 natural gas Substances 0.000 claims description 2
- 125000000962 organic group Chemical group 0.000 claims description 2
- 238000003786 synthesis reaction Methods 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims 2
- 239000000908 ammonium hydroxide Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 150000004696 coordination complex Chemical class 0.000 claims 1
- OUDSFQBUEBFSPS-UHFFFAOYSA-N ethylenediaminetriacetic acid Chemical compound OC(=O)CNCCN(CC(O)=O)CC(O)=O OUDSFQBUEBFSPS-UHFFFAOYSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 abstract description 3
- 239000002738 chelating agent Substances 0.000 description 19
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 14
- 239000001257 hydrogen Substances 0.000 description 14
- 229910052739 hydrogen Inorganic materials 0.000 description 14
- 230000015556 catabolic process Effects 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000006731 degradation reaction Methods 0.000 description 11
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 11
- 230000001590 oxidative effect Effects 0.000 description 11
- 238000010521 absorption reaction Methods 0.000 description 9
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical class NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 7
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 7
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- -1 iron ion Chemical class 0.000 description 6
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 5
- 229960001484 edetic acid Drugs 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 229910021538 borax Inorganic materials 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000797 iron chelating agent Substances 0.000 description 3
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 3
- 235000010339 sodium tetraborate Nutrition 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- 108010008488 Glycylglycine Proteins 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 230000003139 buffering effect Effects 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000005188 flotation Methods 0.000 description 2
- 238000002309 gasification Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 229960002449 glycine Drugs 0.000 description 2
- 235000013905 glycine and its sodium salt Nutrition 0.000 description 2
- 229940075525 iron chelating agent Drugs 0.000 description 2
- 150000002506 iron compounds Chemical class 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 238000006864 oxidative decomposition reaction Methods 0.000 description 2
- 238000010525 oxidative degradation reaction Methods 0.000 description 2
- 229960003330 pentetic acid Drugs 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LMSDCGXQALIMLM-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid;iron Chemical compound [Fe].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O LMSDCGXQALIMLM-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- NJMVHBQEIKOPIT-UHFFFAOYSA-N acetic acid 2-(2-aminoethylamino)ethanol Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.NCCNCCO NJMVHBQEIKOPIT-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 101150015779 act3 gene Proteins 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- SSJXIUAHEKJCMH-UHFFFAOYSA-N cyclohexane-1,2-diamine Chemical compound NC1CCCCC1N SSJXIUAHEKJCMH-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- YMAWOPBAYDPSLA-UHFFFAOYSA-N glycylglycine Chemical compound [NH3+]CC(=O)NCC([O-])=O YMAWOPBAYDPSLA-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 235000014413 iron hydroxide Nutrition 0.000 description 1
- NCNCGGDMXMBVIA-UHFFFAOYSA-L iron(ii) hydroxide Chemical compound [OH-].[OH-].[Fe+2] NCNCGGDMXMBVIA-UHFFFAOYSA-L 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 239000011275 tar sand Substances 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/48—Sulfur compounds
- B01D53/52—Hydrogen sulfide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
- B01D53/1493—Selection of liquid materials for use as absorbents
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K1/00—Purifying combustible gases containing carbon monoxide
- C10K1/08—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors
- C10K1/10—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors with aqueous liquids
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Analytical Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Environmental & Geological Engineering (AREA)
- Treating Waste Gases (AREA)
- Gas Separation By Absorption (AREA)
- Industrial Gases (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US857,863 | 1986-05-01 | ||
| US06/857,863 US4774071A (en) | 1986-05-01 | 1986-05-01 | Process and composition for the removal of hydrogen sulfide from gaseous streams |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1288087C true CA1288087C (fr) | 1991-08-27 |
Family
ID=25326885
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000535735A Expired - Fee Related CA1288087C (fr) | 1986-05-01 | 1987-04-28 | Methode et composition pour separer le sulfure d'hydrogene present dans des debits gazeux |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4774071A (fr) |
| EP (1) | EP0244249B1 (fr) |
| JP (1) | JPS62269729A (fr) |
| CN (1) | CN1008071B (fr) |
| AU (1) | AU605764B2 (fr) |
| CA (1) | CA1288087C (fr) |
| DK (1) | DK225387A (fr) |
| NO (1) | NO168231C (fr) |
| NZ (1) | NZ220088A (fr) |
| PH (1) | PH23589A (fr) |
| SU (1) | SU1679970A3 (fr) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4889701A (en) * | 1982-01-04 | 1989-12-26 | Mobil Oil Corporation | Process for oxidizing multivalent metals |
| US5149460A (en) * | 1985-08-23 | 1992-09-22 | Shell Oil Company | Composition for H2 S removal |
| US5149459A (en) * | 1985-08-23 | 1992-09-22 | Shell Oil Company | H2 S removal composition |
| NZ223528A (en) * | 1987-02-19 | 1991-08-27 | Dow Chemical Co | Process and scrubbing solution for removal of h 2 s and/or co 2 from gas streams |
| US4789530A (en) * | 1987-12-09 | 1988-12-06 | Phillips Petroleum Company | Absorption of hydrogen sulfide with an alkali metal ethylenediaminetetraacetate and/or alkali metal nitrilotriacetate |
| US4830838A (en) * | 1988-11-01 | 1989-05-16 | The Dow Chemical Company | Removal of hydrogen sulfide from fluid streams with minimum production of solids |
| US5026503A (en) * | 1989-07-21 | 1991-06-25 | Amoco Corporation | Composition and method for removing hydrogen sulfide from gas streams |
| US5407646A (en) * | 1989-12-05 | 1995-04-18 | The University Of Toronto Innovations Foundation | Dual impeller method and apparatus for effecting chemical conversion |
| DE4117382A1 (de) * | 1991-05-28 | 1992-12-03 | Metallgesellschaft Ag | Verfahren zum regeln des ph-wertes einer sauren waschfluessigkeit |
| DE4130132A1 (de) * | 1991-09-07 | 1993-03-11 | Michael Wolter | Verfahren zur entfernung von schwefelwasserstoff aus stark kohlendioxidhaltigen gasstroemen |
| CA2100294C (fr) * | 1992-07-27 | 2003-08-19 | David Frederick Bowman | Methode pour eliminer l'hydrogene sulfure dans un melange gazeux |
| US5549789A (en) * | 1992-08-28 | 1996-08-27 | The United States Of America As Represented By The Secretary Of Agriculture | Oxidation of lignin and polysaccharides mediated by polyoxometalate treatment of wood pulp |
| NL9401036A (nl) * | 1994-06-23 | 1996-02-01 | Tno | Anaerobe verwijdering van zwavelverbindingen uit afvalwater. |
| US5543122A (en) * | 1994-11-09 | 1996-08-06 | The Dow Chemical Company | Process for the removal of h2 S from non-condensible gas streams and from steam |
| US5958360A (en) * | 1997-02-07 | 1999-09-28 | Gas Research Institute | Absorber for liquid redox processes |
| GB2369310A (en) * | 2000-09-29 | 2002-05-29 | Fluid Technologies | Removal of contaminants from gas stream using acidic scrubber and oxidation |
| US8034231B2 (en) * | 2008-02-20 | 2011-10-11 | Baker Hughes Incorporated | Method for reducing hydrogen sulfide evolution from asphalt |
| CA2916611C (fr) * | 2013-07-12 | 2018-06-26 | Ihi Corporation | Dispositif d'epuration de gaz d'echappement et systeme de recuperation de co2 |
| US9783458B2 (en) * | 2014-01-31 | 2017-10-10 | Innophos, Inc. | Hydrogen sulfide scavenger |
| CN106103659B (zh) * | 2014-03-17 | 2018-07-06 | 株式会社可乐丽 | 含硫化合物除去用的组合物 |
| CN104437085B (zh) * | 2014-12-26 | 2017-01-25 | 中南大学 | 一种液相高效还原再生脱硝铁基螯合剂的方法 |
| CN106395756B (zh) * | 2016-08-31 | 2018-08-31 | 华陆工程科技有限责任公司 | 一种处理含氨、羰基硫、硫化氢酸性气,并进行硫磺回收的新型工艺 |
| CN109622038A (zh) * | 2018-12-14 | 2019-04-16 | 长春东狮科贸实业有限公司 | 一种用于脱除硫化氢的抑盐脱硫催化剂 |
| CN112275048A (zh) * | 2020-10-15 | 2021-01-29 | 吉林建筑大学 | 一种大气污染的净化与处理装置 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB999800A (en) * | 1962-03-13 | 1965-07-28 | Humphreys & Glasgow Ltd | Purification of gases |
| US4091073A (en) * | 1975-08-29 | 1978-05-23 | Shell Oil Company | Process for the removal of H2 S and CO2 from gaseous streams |
| US4076621A (en) * | 1976-03-15 | 1978-02-28 | Air Resources, Inc. | Chelate oxidation of hydrogen sulfide in sour water |
| US4388293A (en) * | 1981-11-24 | 1983-06-14 | Shell Oil Company | H2 S Removal |
| US4455287A (en) * | 1982-03-15 | 1984-06-19 | Ari Technologies, Inc. | Method of stabilizing chelated polyvalent metal solutions |
| US4532118A (en) * | 1984-03-29 | 1985-07-30 | Kimura Chemical Plants Co., Ltd. | Process for removal of hydrogen sulfide from gases |
| IN166496B (fr) * | 1984-12-24 | 1990-05-19 | Shell Int Research | |
| US4664902A (en) * | 1985-08-23 | 1987-05-12 | Shell Oil Company | Recovery of sulfur from a solid sulfur-containing solution of solubilized iron chelate of nitrilotriacetic acid |
| IN168471B (fr) * | 1985-08-23 | 1991-04-13 | Shell Int Research |
-
1986
- 1986-05-01 US US06/857,863 patent/US4774071A/en not_active Expired - Lifetime
-
1987
- 1987-04-24 NZ NZ220088A patent/NZ220088A/xx unknown
- 1987-04-28 CA CA000535735A patent/CA1288087C/fr not_active Expired - Fee Related
- 1987-04-29 PH PH35197A patent/PH23589A/en unknown
- 1987-04-29 AU AU72199/87A patent/AU605764B2/en not_active Ceased
- 1987-04-30 CN CN87103152.3A patent/CN1008071B/zh not_active Expired
- 1987-04-30 EP EP87303894A patent/EP0244249B1/fr not_active Expired - Lifetime
- 1987-04-30 JP JP62104837A patent/JPS62269729A/ja active Pending
- 1987-04-30 SU SU874202504A patent/SU1679970A3/ru active
- 1987-04-30 NO NO871807A patent/NO168231C/no unknown
- 1987-05-01 DK DK225387A patent/DK225387A/da not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| DK225387D0 (da) | 1987-05-01 |
| PH23589A (en) | 1989-09-11 |
| EP0244249B1 (fr) | 1995-09-20 |
| AU605764B2 (en) | 1991-01-24 |
| NO871807D0 (no) | 1987-04-30 |
| NO168231C (no) | 1992-01-29 |
| CN1008071B (zh) | 1990-05-23 |
| DK225387A (da) | 1987-11-02 |
| SU1679970A3 (ru) | 1991-09-23 |
| EP0244249A3 (en) | 1989-02-22 |
| EP0244249A2 (fr) | 1987-11-04 |
| US4774071A (en) | 1988-09-27 |
| NO168231B (no) | 1991-10-21 |
| AU7219987A (en) | 1987-11-05 |
| CN87103152A (zh) | 1987-12-23 |
| NO871807L (no) | 1987-11-02 |
| NZ220088A (en) | 1990-10-26 |
| JPS62269729A (ja) | 1987-11-24 |
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